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255866

Sigma-Aldrich

2-(1-Cyclohexenyl)ethylamine

97%

Synonym(s):

1-Cyclohexene-1-ethanamine

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About This Item

Linear Formula:
C6H9CH2CH2NH2
CAS Number:
3399-73-3
Molecular Weight:
125.21
EC Number:
222-267-4
MDL number:
MFCD00012058
UNSPSC Code:
12352100
PubChem Substance ID:
24855489
NACRES:
NA.22

Quality Level

200

Assay

97%

refractive index

n20/D 1.4865 (lit.)

bp

53-54 °C/2.5 mmHg (lit.)

density

0.898 g/mL at 25 °C (lit.)

functional group

amine

SMILES string

NCCC1=CCCCC1

InChI

1S/C8H15N/c9-7-6-8-4-2-1-3-5-8/h4H,1-3,5-7,9H2

InChI key

IUDMXOOVKMKODN-UHFFFAOYSA-N

Application

2-(1-Cyclohexenyl)ethylamine has been employed:
  • as substrate for allylic hydroxylation reaction[1]
  • in preparation of thin films and single crystals of 2-(1-cyclohexenyl)ethyl ammonium lead iodide, used to fabricate optoelectronic-compatible heterostructures[2]

Pictograms

FlameCorrosion
GHS02,GHS05

Signal Word

Danger

Hazard Statements

H226,H314

Hazard Classifications

Flam. Liq. 3 - Skin Corr. 1B

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

136.4 °F - closed cup

Flash Point(C)

58 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCBW0173
BCBN4635V
1442236V
1442236
10701HH

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Phenethylammonium iodide

Sigma-Aldrich

805904

Phenethylammonium iodide

K Pradeesh et al.
Optics express, 17(24), 22171-22178 (2009-12-10)
Optoelectronic-compatible heterostructures are fabricated from layered inorganic-organic multiple quantum wells (IO-MQW) of Cyclohexenyl ethyl ammonium lead iodide, (C(6)H(9)C(2)H(4)NH(3))(2)PbI(4) (CHPI). These hybrids possess strongly-resonant optical features, are thermally stable and compatible with hybrid photonics assembly. Room-temperature strong-coupling is observed when these
Facile stereoselective allylic hydroxylation by dopamine. beta.-monooxygenase.
Sirimanne SR and May SW.
Journal of the American Chemical Society, 110(22), 7560-7561 (1988)
S R Sirimanne et al.
The Biochemical journal, 306 ( Pt 1), 77-85 (1995-02-15)
The reaction of dopamine beta-monooxygenase (DBM; EC 1.14.17.1) with the prototypical non-conjugated olefinic substrate, 2-(1-cyclohexenyl)ethylamine (CyHEA) [see Sirimanne and May (1988) J. Am. Chem. Soc. 110, 7560-7561], was characterized. CyHEA undergoes facile DBM-catalysed allylic hydroxylation to form (R)-2-amino-1-(1-cyclohexenyl)ethanol (CyHEA-OH) without

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